L-thereonine producing bacterium belonging to the genus Escherichia and method for producing L-threonine

Active Publication Date: 2005-06-09
AJINOMOTO CO INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0014] An object of present invention is to enhance the productivity of L-threonine-pr

Problems solved by technology

However, there has been no report to date of using a bacterium belonging to the genus Escherichia

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

Cloning of asd Gene from E. coli into pM Vector

[0073] The asd gene was cloned from chromosomal DNA of the E. coli strain (K12 Mu cts62 Mud5005) (VKPM B-6804) obtained from Russian National Collection of Industrial Microorganisms (VKPM) (Dorozhny proezd. 1, Moscow 113545, Russian Federation). First, mini-Mu phage in the E. coli strain (K12 Mu cts62 Mud5005) (VKPM B-6804) was induced. Then, the set of obtained derivatives of plasmids pMud5005 containing parts of chromosome was used for transformation of asd− strain SH 309. The strain SH 309 (VKPM B-3899) obtained from Russian National Collection of Industrial Microorganisms (VKPM) (Dorozhny proezd. 1, Moscow 113545, Russian Federation) has the following phenotype: F− araD139 rpsL150 deoC1 ptsF25 relA1 feb5301 rbsR ugpA704::Tn10 Del (argF-lac) U169 Del (mal-asd) TetR StrR. The asd− strain SH 309 cannot grow on L-medium and requires diaminopimelinic acid (DAPA) for growth. SH 309 asd+ clones harboring plasmid pMud5005-asd were selected...

example 2

Effect of the asd Gene Amplification on Threonine Production

[0075] Both E. coli strains B-3996 and B-3996(pMW-asd) were grown for 18-24 hours at 37° C. on L-agar plates containing streptomycin (100 μg / ml) and ampicillin (100 μg / ml). To obtain seed culture, the strain was grown on a rotary shaker (250 rpm) at 32° C. for 18 hours in 20×200 mm test tubes containing 2 ml of L-broth with 4% sucrose. Then, the fermentation medium was inoculated with 0.1 ml (5%) seed material. The fermentation was performed in 2 ml of minimal medium for fermentation in 20×200 mm test tubes. Cells were grown for 24 hours at 32° C. with shaking at 250 rpm.

[0076] After cultivation, the amount of accumulated L-threonine in the medium was determined by TLC. Sorbfil plates (Stock Company Sorbopolymer, Krasnodar, Russia) were developed with a mobile phase: propan-2-ol:acetone:water:25% aqueous ammonia=25:25:7:6 (v / v). A solution (2%) of ninhydrin in acetone was used as a visualizing reagent. The results are pre...

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PUM

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Abstract

There is disclosed a method for producing L-threonine using bacterium belonging to the genus Escherichia wherein the bacterium has been modified to enhance an activity of aspartate-β-semialdehyde dehydrogenase.

Description

[0001] This application claims priority under 35 U.S.C. §119(e) to provisional application 60 / 586,222, filed on Jul. 9, 2004.BACKGROUND OF THE INVENTION [0002] 1. Technical field [0003] The present invention relates to a method for producing an L-amino acid by fermentation, and more specifically to a gene derived from Escherichia coli which aids in this fermentation. The gene is useful for improvement of L-amino acid production, and specifically, for example, for L-threonine production. [0004] 2. Description of the Related Art [0005] Conventionally, L-amino acids are industrially produced by fermentation methods utilizing strains of microorganisms obtained from natural sources or mutants thereof, which are modified to enhance production yields of L-amino acids. [0006] Many techniques to enhance production yields of L-amino acids have been reported, including transformation of microorganisms with recombinant DNA (see, for example, U.S. Pat. No. 4,278,765). Other techniques for enhanc...

Claims

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Application Information

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IPC IPC(8): C12N1/21C12N9/02C12P13/08C12R1/19
CPCC12P13/08C12N9/0008
Inventor AKHVERDIAN, VALERYSAVRASOVA, EKATERINAKAPLAN, ALLALOBANOV, ANDREYKOZLOV, YURI
Owner AJINOMOTO CO INC
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